NEW SYNTHESIS OF DL-α-AMINOACIDS FROM t-BUTYL N(DIPHENYLMETHYLENE) OXAMATE

DOI: 10.1016/S0040-4039(00)99404-8

Source and publish data:

Tetrahedron Letters p. 3065 - 3068 (1989)

Update date:2022-08-05

Topics:

Authors:

Bazureau, J.P.

Person, D.

Corre, M. Le

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Article abstract of DOI:10.1016/S0040-4039(00)99404-8

The condensation of phosphorus ylids with t-butyl N(diphenylmethylene) oxamate gives 2-aza 1,3-dienes ; subsequent reduction with sodium cyanoborohydride provides protected α-aminoacids.

Full text of DOI:10.1016/S0040-4039(00)99404-8

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Article Doi

NEW SYNTHESIS OF DL-α-AMINOACIDS FROM t-BUTYL N(DIPHENYLMETHYLENE) OXAMATE

DOI: 10.1016/S0040-4039(00)99404-8

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)99404-8

Full text of DOI:10.1016/S0040-4039(00)99404-8

Products guided by the article

R&D Labs maybe for 126181-28-0

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Intramolecular transformation of 2-benzylideneaminoethoxybenzo[d]-1,3,2- dioxaphosphorin-4-one into 3,4-benzo-10-phenyl-1-aza-5,7-dioxa-6-phosphabicyclo- [4.3.1]decane-2,6-dione

Synthesis, X-structure and solvent induced electronic states tuning of meso-tris(4-nitrophenyl)corrolato-copper complex

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